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Home › Dataset Library › Transcription profiling of human CD4+ memory T cells reveals they are preferential targets for bystander activation and apoptosis

Dataset: Transcription profiling of human CD4+ memory T cells reveals they are preferential targets for bystander activation and apoptosis

There is much evidence that T cells may be activated via mechanisms which act independently of direct TCR ligation. Despite this, the...

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There is much evidence that T cells may be activated via mechanisms which act independently of direct TCR ligation. Despite this, the question of whether such forms of ‘bystander’ T cell activation occur during immune responses is hotly debated. To address some outstanding questions, we set up an in vitro system within which to analyse bystander T cell activation in human T cells, in the absence of the possibility for TCR cross-reactivity. In addition, we have investigated the genetic, phenotypic, and functional characteristics of bystander activated T cells. Here, we show that bystander T cell activation is, indeed, observed during a specific immune response, and that it occurs preferentially amongst CD4+ memory T cells. Furthermore, bystander activated T cells display a distinct gene expression profile. The mechanism for bystander T cell activation involves soluble factors, and the outcome is an elevated level of apoptosis. This may provide an explanation for the attrition of T cell memory pools of heterologous specificity during immune responses to pathogens such as viruses. Experiment Overall Design: Three conditions tested with 4 biological repilicates in each: Experiment Overall Design: Resting cells - cells expressing a TCR which does not specifically recognize SEB (Vβ13.1 T cells) and did not upregulate the activation marker CD25 in response to transwell SEB-stimulated co-culture over a 5 day period. Experiment Overall Design: Bystander activated cells - cells expressing a TCR which does not specifically recognize SEB (Vβ13.1 T cells), but which did upregulate the activation marker CD25 in response to transwell SEB-stimulated co-culture over a 5 day period. Experiment Overall Design: Directly activated cells - cells expressing a TCR which is known to specifically recognize SEB (Vβ17 T cells), and which did upregulate the activation marker CD25 in response to direct SEB stimulation over a 5 day period.

Species:
human

Samples:
12

Source:
E-GEOD-13738

PubMed:
19201849

Updated:
Dec.12, 2014

Registered:
Sep.11, 2014


Factors: (via ArrayExpress)
Sample
GSE13738GSM345232
GSE13738GSM345246
GSE13738GSM345250
GSE13738GSM345259
GSE13738GSM345264
GSE13738GSM345266
GSE13738GSM345267
GSE13738GSM345280
GSE13738GSM345281
GSE13738GSM345282
GSE13738GSM345283
GSE13738GSM345284

Tags

  • cell

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